Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 891 recalls have been distributed to District of Columbia in the last 12 months.
Showing 45561–45580 of 47,654 recalls
Recalled Item: TriVascular brand Fill Polymer Kit Recalled by Trivascular, Inc Due to...
The Issue: Selected lots of the Fill Polymer Kit (European Model Number: TVFP14- B) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Necon 10/11 (norethindrone and ethinyl estradiol) Tablets USP Recalled by...
The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenchent (norethindrone and ethinyl estradiol) Tablets USP Recalled by...
The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lutera (levonorgestrel and ethinyl estradiol) Tablets USP Recalled by Watson...
The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zovia (ethynodiol diacetate and ethinyl estradiol) Tablets USP Recalled by...
The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Necon 1/35-28 (norethindrone and ethinyl estradiol) Tablets USP Recalled by...
The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4.5mm PLEO Osteotomy Guide. OrthoPediatrics Corp. markets a pediatric...
The Issue: Complaint received from sales representative that the drill guide tubes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 16 Multi-Sliced CT Scanner System Recalled by Philips And Neusoft...
The Issue: The four screws that secure the patient table top to the carrier pulled out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injections Recalled by Biomerieux Inc Due to The firm...
The Issue: The firm inventoried and distributed 0.9% Sodium Chloride Saline bags as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peanuts in Shell Recalled by Energy Club Inc Due to Potential Salmonella...
The Issue: Trifecta Foods, LLC in Pacoima, CA is voluntarily recalling products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Peanuts in Shell Recalled by Energy Club Inc Due to Potential Salmonella...
The Issue: Trifecta Foods, LLC in Pacoima, CA is voluntarily recalling products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Green & Black's Organic Peanut & Sea Salt Milk Chocolate Recalled by...
The Issue: Mondelez Global LLC (Mondelez Global) is voluntarily recalling the U.S....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PureFit Peanut Butter Bars Recalled by PureFit Inc Due to Potential...
The Issue: PureFit is recalling PureFit Peanut Butter Crunch Bars because of possible...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal...
The Issue: Thirty fetal scalp electrodes were found to have an incomplete package seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HX2 Temp Manage SYS 120V The Terumo HX2 Temperature Management Recalled by...
The Issue: Based on a retrospective review of quality data, AC Control boards used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tested AC Control BD Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Based on a retrospective review of quality data, AC Control boards used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invivo Corporation Expression MRI Patient Monitoring System. The Expression...
The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRT-1504/A4 - Titan X MRI System MRT-30 I0A/5 - Titan Recalled by Toshiba...
The Issue: It was found that there is a problem with the LCD monitor used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The HINES package is a cello/poly laminated bag Recalled by Hines Nut Co Due...
The Issue: Hines Nut Company Inc. recalled its SALTED JUMBO VIRGINIA IN-SHELL PEANUTS....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral Recalled...
The Issue: OSSUR is recalling the Symbionic Leg because it is not recognizing the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.